Real-Time PCR Identification of Unique Bacillus anthracis Sequences
Language English Country Czech Republic Media print
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
26667574
DOI
10.14712/fb2015061050178
PII: file/5789/fb2015a0024.pdf
Knihovny.cz E-resources
- MeSH
- Antigens, Bacterial genetics MeSH
- Bacillus anthracis genetics isolation & purification pathogenicity MeSH
- Bacillus cereus genetics pathogenicity MeSH
- Bacterial Proteins genetics MeSH
- Bacterial Toxins genetics MeSH
- DNA, Bacterial analysis MeSH
- Virulence Factors genetics MeSH
- Genetic Markers MeSH
- Real-Time Polymerase Chain Reaction MeSH
- Plasmids genetics MeSH
- Sensitivity and Specificity MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- anthrax toxin MeSH Browser
- Antigens, Bacterial MeSH
- Bacterial Proteins MeSH
- Bacterial Toxins MeSH
- DNA, Bacterial MeSH
- Virulence Factors MeSH
- Genetic Markers MeSH
Bacillus anthracis is a spore-forming, Gram-positive microorganism. It is a causative agent of anthrax, a highly infectious disease. It belongs to the "Bacillus cereus group", which contains other closely related species, including Bacillus cereus, Bacillus thuringiensis, Bacillus mycoides, Bacillus weihenstephanensis, and Bacillus pseudomycoides. B. anthracis naturally occurs in soil environments. The BA5345 genetic marker was used for highly specific detection of B. anthracis with TaqMan probes. The detection limit of a real-time PCR assay was estimated at the level of 16.9 copies (CI95% - 37.4 to 37.86, SD = 0.2; SE = 0.118). Oligonucleotides designed for the targeted sequences (within the tested locus) revealed 100 % homology to B. anthracis strain reference sequences deposited in the database (NCBI) and high specificity to all tested B. anthracis strains. Additional in silico analysis of plasmid markers pag and cap genes with B. anthracis strains included in the database was carried out. Our study clearly indicates that the BA5345 marker can be used with success as a chromosomal marker in routine identification of B. anthracis; moreover, detection of plasmid markers indicates virulence of the examined strains.
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